Canonical Allele Identifier: CA2450541994

Gene: COL4A6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108157240C= , CM000685.2:g.108157240C=	GRCh38
NC_000023.10:g.107400470C= , CM000685.1:g.107400470C=	GRCh37
NC_000023.9:g.107287126C=	NCBI36
NG_012059.2:g.287235G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334504.12:c.4833G= MANE Select	ENSP00000334733.7:p.Glu1611=
ENST00000334504.11:c.4833G=	ENSP00000334733.7:p.Glu1611=
ENST00000372216.8:c.4836G=	ENSP00000361290.4:p.Glu1612=
ENST00000394872.6:c.4884G=	ENSP00000378340.3:p.Glu1628=
ENST00000538570.5:c.4662G=	ENSP00000445236.1:p.Glu1554=
ENST00000545689.2:c.4797G=	ENSP00000443707.2:p.Glu1599=
ENST00000621266.4:c.4761G=	ENSP00000482970.1:p.Glu1587=
NM_001287758.1:c.4884G=	NP_001274687.1:p.Glu1628=
NM_001287759.1:c.4761G=	NP_001274688.1:p.Glu1587=
NM_001287760.1:c.4662G=	NP_001274689.1:p.Glu1554=
NM_001847.3:c.4836G=	NP_001838.2:p.Glu1612=
NM_033641.3:c.4833G=	NP_378667.1:p.Glu1611=
XM_006724617.2:c.4887G=	XP_006724680.1:p.Glu1629=
XM_011530852.1:c.4815G=	XP_011529154.1:p.Glu1605=
XM_011530853.1:c.4803G=	XP_011529155.1:p.Glu1601=
XM_006724617.3:c.4887G=	XP_006724680.1:p.Glu1629=
XM_011530852.2:c.4815G=	XP_011529154.1:p.Glu1605=
XM_011530853.3:c.4803G=	XP_011529155.1:p.Glu1601=
NM_001847.4:c.4836G=	NP_001838.2:p.Glu1612=
NM_033641.4:c.4833G= MANE Select	NP_378667.1:p.Glu1611=
NM_001287758.2:c.4884G=	NP_001274687.1:p.Glu1628=
NM_001287759.2:c.4761G=	NP_001274688.1:p.Glu1587=
NM_001287760.2:c.4662G=	NP_001274689.1:p.Glu1554=